Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580606Generated: November 4, 2026

Bromazepam → 7-bromo-2,3-dihydro-2-oxo-5-(2-pyridyl)-1H-1,4-benzodiazepin-1-acetic acid methyl ester

https://huagongshe.com/reaction/1580606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromazepamHCID 2441—
ReactantDimethylformamideHCID 6228—
ReactantMethyl bromoacetateHCID 60984—
ReactantSodium MethoxideHCID 10942334—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product7-bromo-2,3-dihydro-2-oxo-5-(2-pyridyl)-1H-1,4-benzodiazepin-1-acetic acid methyl esterHCID 54526215—

Reaction Steps

A mixture of 0.1 mole of 7-bromo-1,3-dihydro-5-(2-pyridyl)-2H-1,4-benzodiazepin-2-one and 0.11 mole of sodium methoxide in about 200 ml. of dimethylformamide is heated at about 95° c. for about 20 minutes. To the mixture is added a solution of 0.11 mole of methyl bromoacetate in about 200 ml. of toluene over a period of about 1 hour at about 95° C., and heating is continued for an additional period of about 6 hours. The reaction mixture is then evaporated in vacuo and the residue thus obtained is stirred with about 500 ml. of water. The resulting suspension is filtered and the solids thus obtained are crystallized from a suitable organic solvent such as ether, methanol, methylene chloride, methylene chloridemethanol and the like to obtain 7-bromo-2,3-dihydro-2-oxo-5-(2-pyridyl)-1H-1,4-benzodiazepin-1-acetic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03933816
Source datasetuspto-grants-1976_01
ORD IDord-5c59a8a07fd24e6195b2d36fa8a49e97
Source noteuspto-grants-1976_01